Allele Registry

Canonical Allele Identifier: PA2580124518

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000012954

RCV003234903

ClinVar Variation:

12172

HGVS (amino-acid)	Matching Registered Transcripts
NP_000491.4:p.Glu381Asp	CA3732657 NM_000500.9:c.1143G>C CA363511265 NM_000500.9:c.1143G>T